Department of Medical Biochemistry, Graduate School of Medicine, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-85823, Japan.
J Biochem. 2011 May;149(5):495-7. doi: 10.1093/jb/mvr022. Epub 2011 Feb 15.
GPR55 is a seven transmembrane G protein-coupled receptor and was originally identified as a putative third cannabinoid receptor. Recently, lysophosphatidylinositol (LPI) was reported to be a GPR55 ligand. Stimulation of GPR55 by LPI activates G(12/13) and G(q/11) proteins, induces phosphorylation of the extracellular signal-regulated kinase and increases intracellular calcium concentration. Lysophospholipids are molecularly quite diverse across species and tissues. A recent report showed that the predominant fatty acyl moiety of LPI in rat brain is stearic acid followed by arachidonic acid. The biological activity of arachidonic acid-containing LPI species towards GPR55 was shown to be markedly higher than that of LPI species containing other fatty acyl groups, suggesting that 2-arachidonolyl LPI is the most likely natural ligand of GPR55.
GPR55 是一种七次跨膜 G 蛋白偶联受体,最初被鉴定为一种假定的第三大麻素受体。最近,溶血磷脂酰肌醇(LPI)被报道为 GPR55 的配体。LPI 对 GPR55 的刺激激活 G(12/13) 和 G(q/11) 蛋白,诱导细胞外信号调节激酶的磷酸化并增加细胞内钙离子浓度。溶血磷脂在物种和组织之间具有相当大的分子多样性。最近的一份报告表明,大鼠脑中 LPI 的主要脂肪酸酰基部分是硬脂酸,其次是花生四烯酸。含有花生四烯酸的 LPI 对 GPR55 的生物活性明显高于含有其他脂肪酸酰基的 LPI 物种,表明 2-花生四烯酰基 LPI 可能是 GPR55 的天然配体。